“…Over the last two decades, visible light photocatalysis has emerged as a greener approach in organic synthesis. 20 Also, the replacement of volatile organic compounds (VOCs) as solvents with greener media 21 like water 22 has become a need of the day. In line with our current research interest in green chemistry and photoredox catalysis, herein we report an efficient and inexpensive visible light-mediated organocatalysed synthesis of diazenyl compounds using 1,3-diones and aryl diazonium salts without the use of any metal activator or ligand.…”
“…Over the last two decades, visible light photocatalysis has emerged as a greener approach in organic synthesis. 20 Also, the replacement of volatile organic compounds (VOCs) as solvents with greener media 21 like water 22 has become a need of the day. In line with our current research interest in green chemistry and photoredox catalysis, herein we report an efficient and inexpensive visible light-mediated organocatalysed synthesis of diazenyl compounds using 1,3-diones and aryl diazonium salts without the use of any metal activator or ligand.…”
“…2–7 Consequently, much effort has been dedicated to developing efficient strategies for the introduction of the thiocyanato group into molecules. 8 Despite their importance, there has been limited progress in the synthesis of aryl thiocyanates. Synthetic strategies that have been developed include nucleophilic or electrophilic thiocyanations of aryl substrates such as arenes, 9 aryl halides, 10 organometallic nucleophiles, 11 arylboron compounds 12 and aryl diazonium salts (Scheme 1a, left).…”
A tandem electrophilic thiocyanation/carbocyclization of alkynes has been developed, affording thiocyanato-substituted phenanthrenes, dihydronaphthalenes, 2H-chromenes and dihydroquinolines in moderate to excellent yields.
“…It also plays a very important role in organic synthesis, for example, the synthesis of sulfur-containing nitriles − and nitrogen- or sulfur-containing heterocycles . Therefore, the study on the synthesis of organic thiocyanates is of great importance, and a series of effective and practical protocols were developed in recent years . The selections of the reaction partners and the catalytic system are often the key issues for this purpose.…”
A novel electrochemical cross-coupling method for the
synthesis
of thiocyanates via the direct cyanation of readily
available thiophenols or thiols with trimethylsilyl cyanide (TMSCN)
was developed. This approach was also suitable for selenols. External
oxidant-free, transition-metal-free and mild operating conditions
were the main advantages of this protocol. A series of thiocyanates
and selenocyanates could be obtained in moderate to high yields.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.